SMCHD1 mutations cause FSHD type 2 and act as modifiers of disease severity

M. Larsen; W. Kress; S. Rost; N. El Hajj; C. R. Mueller

doi:10.1016/j.nmd.2014.06.025

SMCHD1 mutations cause FSHD type 2 and act as modifiers of disease severity

M. Larsen
, W. Kress
, S. Rost
, N. El Hajj
, C. R. Mueller

University of Wurzburg

Research output: Contribution to journal › Meeting Abstract › peer-review

Original language	English
Pages (from-to)	797-797
Number of pages	1
Journal	Neuromuscular Disorders
Volume	24
Issue number	9-10
DOIs	https://doi.org/10.1016/j.nmd.2014.06.025
Publication status	Published - Oct 2014
Externally published	Yes
Event	19th International Congress of the World-Muscle-Society - Berlin, Germany Duration: 7 Oct 2014 → 11 Oct 2014

Access to Document

10.1016/j.nmd.2014.06.025

Cite this

@article{06ac004be4584f90b0401efce531ad78,

title = "SMCHD1 mutations cause FSHD type 2 and act as modifiers of disease severity",

author = "M. Larsen and W. Kress and S. Rost and \{El Hajj\}, N. and Mueller, \{C. R.\}",

year = "2014",

month = oct,

doi = "10.1016/j.nmd.2014.06.025",

language = "English",

volume = "24",

pages = "797--797",

journal = "Neuromuscular Disorders",

issn = "0960-8966",

publisher = "Elsevier Ltd",

number = "9-10",

note = "19th International Congress of the World-Muscle-Society ; Conference date: 07-10-2014 Through 11-10-2014",

}

TY - JOUR

T1 - SMCHD1 mutations cause FSHD type 2 and act as modifiers of disease severity

AU - Larsen, M.

AU - Kress, W.

AU - Rost, S.

AU - El Hajj, N.

AU - Mueller, C. R.

PY - 2014/10

Y1 - 2014/10

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=hbku_researchportal&SrcAuth=WosAPI&KeyUT=WOS:000342870200022&DestLinkType=FullRecord&DestApp=WOS_CPL

U2 - 10.1016/j.nmd.2014.06.025

DO - 10.1016/j.nmd.2014.06.025

M3 - Meeting Abstract

SN - 0960-8966

VL - 24

SP - 797

EP - 797

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

IS - 9-10

T2 - 19th International Congress of the World-Muscle-Society

Y2 - 7 October 2014 through 11 October 2014

ER -

SMCHD1 mutations cause FSHD type 2 and act as modifiers of disease severity

Access to Document

Other files and links

Cite this